rs879255442

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CA)	6	BRCA2 variant considered pathogenic for breast cancer
(AC;AC)	0	common in clinvar
(CA;CA)	0	common/normal

Make rs879255442(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32336599

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs879255442
dbSNP (classic)	rs879255442
ClinGen	rs879255442
ebi	rs879255442
HLI	rs879255442
Exac	rs879255442
Gnomad	rs879255442
Varsome	rs879255442
LitVar	rs879255442
Map	rs879255442
PheGenI	rs879255442
Biobank	rs879255442
1000 genomes	rs879255442
hgdp	rs879255442
ensembl	rs879255442
geneview	rs879255442
scholar	rs879255442
google	rs879255442
pharmgkb	rs879255442
gwascentral	rs879255442
openSNP	rs879255442
23andMe	rs879255442
SNPshot	rs879255442
SNPdbe	rs879255442
MSV3d	rs879255442
GWAS Ctlg	rs879255442

Max Magnitude

6

ClinVar
Risk	rs879255442(-;-)
Alt	rs879255442(-;-)
Reference	Rs879255442(AC;AC)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910736_32910737delCA
CLNSRC
CLNACC	RCV000238671.2,